Taiwan FDA registration 0746eca6224c76ed0f25816f4ec64da4
"Kehui" three-row sewing coupling type end-to-end ring-shaped sewing device
TW: “柯惠”三排縫合釘式端對端環形縫合器
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Aug 30, 2024 – Aug 30, 2029ActiveRegistration details
- Analysis ID
- 0746eca6224c76ed0f25816f4ec64da4
- Customs Code
- DHA05603738309
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4750 Implantable Joints
- Import Information
- import
Dates and status
- Registration Date
- Aug 30, 2024
- Expiry Date
- Aug 30, 2029
About this record
Access comprehensive regulatory information for "Kehui" three-row sewing coupling type end-to-end ring-shaped sewing device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0746eca6224c76ed0f25816f4ec64da4 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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